chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	46125302	46125303	T	G	12	GENIC	homozygous	136094110
2	46125306	46125307	T	A	13	GENIC	homozygous	403000277
2	46125306	46125307	T	C	13	GENIC	heterozygous	403000278
2	46125309	46125310	T	C	14	GENIC	homozygous	136094111
2	46125313	46125314	C	A	15	GENIC	homozygous	136094112
2	46125314	46125315	T	G	15	GENIC	homozygous	136094113
2	46129717	46129718	A	T	38	GENIC	homozygous	153925412
2	46125669	46125671	AT		33	GENIC	homozygous	141323450
2	46126430	46126431	A		33	GENIC	possibly homozygous	135904322
2	46129329	46129329		A	38	GENIC	possibly homozygous	141323451
2	46128943	46128944	T	A	49	GENIC	homozygous	141372717
2	46129717	46129718	A		38	GENIC	heterozygous	403553426